Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,929 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,929 in last 12 months

Showing 2516125180 of 29,228 recalls

Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: DISP 9730950 STRL SPHERE Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PIN Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: Recalled by...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8"x10" Reorder Number: Recalled by...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: TUMOR RESECTION KIT 9733608 SKULL MOUNT Recalled by Medtronic Navigation,...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated Recalled...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: INST 9731132 KIT CR DRIVER 5PK Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: BIOPSY NEEDLE KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PAK 9733497 NAV NIM-SPINE PEDICLE ACC KT Recalled by Medtronic Navigation,...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PATIENT TRACKER 9733534XOM ENT 1PK Recalled by Medtronic Navigation, Inc....

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PIN Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: BAG 9732315 MOUSE STERILE 15 PK Recalled by Medtronic Navigation, Inc. Due...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PACK 9731975 TUMOR RESECTION AXIEM CR Recalled by Medtronic Navigation, Inc....

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: DISP 9730951 STRL SPHERE Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Cenorin, LLC

Recalled Item: HLD Systems Model 610 Washer/High Level Disinfector. Maximum weight of...

The Issue: Cenorin LLC is voluntarily recalling HLD Systems Model 610 Washer/High Level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...

The Issue: System error 01779 is produced when the battery cannot be charged due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...

The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Heraeus Kulzer, LLC.

Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...

The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing